Guaianolide sesquiterpene lactones from Cichorium intybus (Asteraceae)

Citation
Yh. Deng et al., Guaianolide sesquiterpene lactones from Cichorium intybus (Asteraceae), Z NATURFO B, 56(8), 2001, pp. 787-796
Citations number
68
Categorie Soggetti
Chemistry
Journal title
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES
ISSN journal
09320776 → ACNP
Volume
56
Issue
8
Year of publication
2001
Pages
787 - 796
Database
ISI
SICI code
0932-0776(200108)56:8<787:GSLFCI>2.0.ZU;2-0
Abstract
Ten guaianolides, including three previously unreported natural products, w ere isolated from the aerial parts of Cichorium intybus (Asteraceae), more commonly known as chicory. Two of the new compounds (8 and 9) were analogue s of lactupicrin and 11 beta ,13-dihydrolactupicrin, respectively, with the C-15 oxidized to the aldehyde state. The third new natural product, which we have called intybulide A (10), is an isomer of lactucin with the lactone closed to the C-8 oxygen rather than the C-6.